Allele Registry

Canonical Allele Identifier: PA2825769873

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 450303

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Arg1138Cys	CA1706610 NM_001130986.2:c.3412C>T